Corticosteriods Flashcards

1
Q

Define corticosteroids

A

A group of natural and synthetic substances that mimic in part or wholly the actions of the adrenal hormone, cortisol

  • most tx uses based on glucocorticoid actions
  • broad physiological effects: anti-inflammatory mainly
  • therapeutic uses and dose ranges are intertwined
    • Medium doses: anti-inflammatory tx
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2
Q

Why do corticosteroids exhibit a delayed response?

A

Due to the requirement for protein synthesis

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3
Q

Describe tissue selectivity in corticosteroid action

A
  • Aldosterone selectively activates MCR
  • Cortisol binds with equal affinity to MCR/GCR
  • Synthetic agents are designed to have GCR selectivity
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4
Q

What can cause hyperactivation of HPA axis?

A

Hyperadrenocorticism, Cushing’s syndrome - can arise from pituitary tumors or adrenal gland tumors

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5
Q

What is the MOA for stressors to inhibit cortisol synthesis?

A

Stressors inhibit 3-beta-hydroxysteroid dehydrogenase > decr cortisol synthesis (adrenal cortex)

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6
Q

Most physiological actions of corticosteroids are mediated what two classes of receptors?

A

Glucocorticoid receptors (GCR) Mineralcorticoid receptors (MCR)

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7
Q

What 4 paths do pharmacological doses of glucocorticoids evoke actions through?

A

1) genomic responses via cytotoxic GCRs - involves altered protein synth (slow-medium effects) 2) Non-Genomic Responses via cytotoxic GCRs 3) Non-Genomic Responses via membrane-bound GCRs 4) other non specific responses

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8
Q

Glucocorticoid actions

A
  1. Enhanced carb metabolism
  2. Protein catabolism
  3. Mobilizes FA from adipose
  4. Blockade of Inflammatory Cascade (robust doses)
  5. Altered electrolyte and water balance (MCR activation)
  6. CNS effects
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9
Q

Adverse effects of Corticosteroids

A
  1. HPAA suppression (sudden withdrawal - fatal)
  2. Muscle wasting, delayed wound healing, bone loss, thinning of skin (protein catabolism)
  3. Diabetes
  4. Hypothyroidism

**adverse effects correlate with DOSE and DURATION of treatment

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10
Q

Precautions for Glucocorticoid Therapy

A
  • Rx does NOT cure dz
  • use topical if feasible to lessen systemic imbalances
  • use minimal effective dose > prevent Cushing’s
  • use step-down protocols when terminating tx > prevent Addison’s
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11
Q

Contraindications for Glucocorticoids

A
  • untreated pre-existing infections
  • high doses in late stage pregnant animals
  • diabetes mellitus
  • renal dz/insufficiency
  • CHF
  • Young animals
  • GI ulcers or hypersecretory disorders
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12
Q

What are some lab concerns with glucocorticoids?

A
  • Leukopenia, neutrophilia (aka stress leukogram)
  • Thrombocytosis
  • Hyperglycemia
  • Hypercholesterolemia
  • Elevated ALP
  • Dec serum K+
  • Decr thyroid values
  • Suppressed rxn to skin tests/systemic bacterial infxn
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13
Q

What are the four chemical classes of glucocorticoids?

A
  1. Group A (short-acting): hydrocortisone, prednisolone, methylprednisolone, prednisone
  2. Group B (intermediate-acting): triamcinolone
  3. Group C (long-acting): betamethasone, dexmethasone, dexamethasone sodium phosphate
  4. Group D
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14
Q

What two things are associated with the C21 hydroxyl group in glucocorticoids?

A

Incr GCR activity and decr MCR activity

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15
Q

Pharmacokinetics of Glucocorticoids

A
  • most eliminated by hepatic metabolism
  • certain side chains delay metabolism and enhance duration of action
  • many synthetic agents are NOT bound to transcortin - improves speed of cellular penetration/faster action
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16
Q

True or False, pharmacodynamics of corticosteriods matches plasma pharmacokinetics?

A

False; biological action lasts far longer than drug levels in plasma

17
Q

Effects of steroids are modified by what?

A

Their ester form; duration of action of free alcohol or highly soluble esters = biologic T1/2

18
Q

Reasons for High-Dose Steroids

A
  • Prevention of secondary injury: ASCI, ischemia, vasospasm, free radical production
  • Immunosuppressive - CNS inflamm dz